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转移性神经母细胞瘤相关性难治性扩张型心肌病。

Refractory dilated cardiomyopathy associated with metastatic neuroblastoma.

机构信息

Baylor College of Medicine, Houston, Texas, USA.

出版信息

Pediatr Blood Cancer. 2010 Oct;55(4):736-8. doi: 10.1002/pbc.22569.

DOI:10.1002/pbc.22569
PMID:20589652
Abstract

A 2-year-old African American male presented with heart failure and an abdominal mass. Computerized tomography (CT) scan revealed a 7 cm adrenal lesion, confirmed as poorly differentiated neuroblastoma (NB). CT and meta-iodobenzoguanidine (MIBG) scans identified multiple metastases, but cardiac MIBG imaging was absent. Cardiac ejection fraction (EF) was 8% with 7% shortening fraction. The patient underwent six cycles of chemotherapy and investigational immunotherapy. Cardiac function improved to 26% EF. However, the tumor proved unresponsive to treatment. The patient died from stage IV congestive heart failure (CHF) and progressive NB. Autopsy confirmed dilated cardiomyopathy with endocardial fibroelastosis.

摘要

一名 2 岁的非裔美国男性因心力衰竭和腹部肿块就诊。计算机断层扫描(CT)显示 7 厘米的肾上腺病变,被确认为低分化神经母细胞瘤(NB)。CT 和间碘苄胍(MIBG)扫描发现多处转移,但心脏 MIBG 成像缺失。心脏射血分数(EF)为 8%,缩短分数为 7%。患者接受了六轮化疗和试验性免疫治疗。心脏功能改善至 26%的 EF。然而,肿瘤对治疗无反应。患者死于 IV 期充血性心力衰竭(CHF)和进展性 NB。尸检证实为扩张型心肌病伴心内膜弹力纤维增生症。

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Refractory dilated cardiomyopathy associated with metastatic neuroblastoma.转移性神经母细胞瘤相关性难治性扩张型心肌病。
Pediatr Blood Cancer. 2010 Oct;55(4):736-8. doi: 10.1002/pbc.22569.
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Neuroblastoma presenting with dilated cardiomyopathy.以扩张型心肌病为表现的神经母细胞瘤。
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[Dilated cardiomyopathy in childhood: intravital differentiation of endocardial fibroelastosis using transvascular endomyocardial biopsy].[儿童扩张型心肌病:经血管心内膜心肌活检对心内膜弹力纤维增生症的活体鉴别]
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Case report: Catecholamine cardiomyopathy in children with neuroblastoma.病例报告:神经母细胞瘤患儿的儿茶酚胺心肌病
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分泌儿茶酚胺的神经母细胞瘤导致胎儿水肿。
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